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首页> 外文期刊>Cellular Physiology and Biochemistry >Smad Ubiquitination Regulatory Factor 1 (Smurf1) Promotes Thyroid Cancer Cell Proliferation and Migration via Ubiquitin-Dependent Degradation of Kisspeptin-1
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Smad Ubiquitination Regulatory Factor 1 (Smurf1) Promotes Thyroid Cancer Cell Proliferation and Migration via Ubiquitin-Dependent Degradation of Kisspeptin-1

机译:Smad泛素化调节因子1(Smurf1)通过泛素依赖性的Kisspeptin-1降解促进甲状腺癌细胞的增殖和迁移。

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Background/Aims Thyroid cancer is the most common malignancy in human endocrine system. Smad ubiquitination regulatory factor 1 (Smurf1) is an E3 ubiquitin-protein ligase in ubiquitin-proteasome pathway (UPP) system. This study aimed to investigate the effects of Smurf1 on thyroid cancer proliferation and metastasis, as well as underlying potential mechanism. Methods The expression levels of Smurf1 in thyroid tumor tissues and thyroid cancer cells were detected by western blotting and qRT-PCR. Then, the effects of up-regulation or down-regulation of Smurf1 on thyroid cancer cell viability, migration, invasion, proliferation and apoptosis were measured using trypan blue exclusion assay, two-chamber migration (invasion) assay, cell colony formation assay and Guava Nexin assay, respectively. The ubiquitination of kisspeptin-1 (KISS-1) was assessed by protein ubiquitination assay. Finally, the effects of KISS-1 overexpression on activity of nuclear factor-kappa B (NF-κB) signaling pathway, as well as thyroid cancer cell viability, migration, invasion, proliferation and apoptosis were also detected, respectively. Results Smurf1 was highly expressed in thyroid tumor tissues and thyroid cancer cells. Up-regulation of Smurf1 promoted the viability, migration, invasion and proliferation of thyroid cancer cells. Knockdown of Smurf1 had opposite effects. Moreover, smurf1 promoted the ubiquitination of KISS-1. Overexpression of KISS-1 inactivated NF-κB pathway, suppressed thyroid cancer cell viability, migration, invasion and proliferation, and induced cell apoptosis. Conclusion Up-regulation of Smurf1 exerted important roles in thyroid cancer formation and development by promoting thyroid cancer proliferation and metastasis. The ubiquitin-dependent degradation of KISS-1 induced by Smurf1 and the activation of NF-κB signaling pathway might be involved in this process. Smurf1 could be an effective therapy target and biomarker for thyroid cancer treatment.
机译:背景/目的甲状腺癌是人类内分泌系统中最常见的恶性肿瘤。 Smad泛素化调节因子1(Smurf1)是泛素-蛋白酶体途径(UPP)系统中的E3泛素蛋白连接酶。这项研究旨在调查Smurf1对甲状腺癌的增殖和转移的影响,以及潜在的潜在机制。方法采用Western blotting和qRT-PCR检测Smurf1在甲状腺肿瘤组织和甲状腺癌细胞中的表达水平。然后,使用台盼蓝排除法,两室迁移(侵袭)法,细胞集落形成法和番石榴法测定了Smurf1上调或下调对甲状腺癌细胞活力,迁移,侵袭,增殖和凋亡的影响。 Nexin测定法。 Kisspeptin-1(KISS-1)的泛素化通过蛋白质泛素化测定进行评估。最后,还分别检测了KISS-1过表达对核因子-κB(NF-κB)信号通路活性的影响,以及甲状腺癌细胞的活力,迁移,侵袭,增殖和凋亡。结果Smurf1在甲状腺肿瘤组织和甲状腺癌细胞中高表达。 Smurf1的上调促进了甲状腺癌细胞的活力,迁移,侵袭和增殖。击倒Smurf1具有相反的效果。此外,smurf1促进了KISS-1的泛素化。 KISS-1的过表达使NF-κB通路失活,抑制了甲状腺癌细胞的活力,迁移,侵袭和增殖,并诱导了细胞凋亡。结论Smurf1的上调通过促进甲状腺癌的增殖和转移在甲状腺癌的形成和发展中起重要作用。 Smurf1诱导的KISS-1的泛素依赖性降解和NF-κB信号通路的激活可能与该过程有关。 Smurf1可能是甲状腺癌治疗的有效治疗靶点和生物标志物。

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